SRX12798390 GSM5658928 SRP343427 SRS10744150 GSM5658928 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol protocol, followed by DNase treatment. RNA was then re-purified with an aqueous column-based protocol followed by gel analysis to analyze purity and quality of the RNA. The RNAseq libraries were prepared with Illumina's 'TruSeq Stranded mRNAseq Sample Prep kit' (Illumina). Read 1 aligns to the ANTISENSE strand and Read 2 aligns to the SENSE strand. * The libraries were quantitated by qPCR and sequenced on two lanes for 101 cycles from one end of the fragments on a HiSeq 4000 using a HiSeq 4000 sequencing kit version 1. Fastq files were generated and demultiplexed with with the bcl2fastq v2.17.1.14 Conversion Software (Illumina). Illumina HiSeq 4000 gds 305658928 GSM5658928 GEO Accession GSM5658928 SRX12798391 GSM5658929 SRP343427 SRS10744151 GSM5658929 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol protocol, followed by DNase treatment. RNA was then re-purified with an aqueous column-based protocol followed by gel analysis to analyze purity and quality of the RNA. The RNAseq libraries were prepared with Illumina's 'TruSeq Stranded mRNAseq Sample Prep kit' (Illumina). Read 1 aligns to the ANTISENSE strand and Read 2 aligns to the SENSE strand. * The libraries were quantitated by qPCR and sequenced on two lanes for 101 cycles from one end of the fragments on a HiSeq 4000 using a HiSeq 4000 sequencing kit version 1. Fastq files were generated and demultiplexed with with the bcl2fastq v2.17.1.14 Conversion Software (Illumina). Illumina HiSeq 4000 gds 305658929 GSM5658929 GEO Accession GSM5658929 SRX12798392 GSM5658930 SRP343427 SRS10744152 GSM5658930 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol protocol, followed by DNase treatment. RNA was then re-purified with an aqueous column-based protocol followed by gel analysis to analyze purity and quality of the RNA. The RNAseq libraries were prepared with Illumina's 'TruSeq Stranded mRNAseq Sample Prep kit' (Illumina). Read 1 aligns to the ANTISENSE strand and Read 2 aligns to the SENSE strand. * The libraries were quantitated by qPCR and sequenced on two lanes for 101 cycles from one end of the fragments on a HiSeq 4000 using a HiSeq 4000 sequencing kit version 1. Fastq files were generated and demultiplexed with with the bcl2fastq v2.17.1.14 Conversion Software (Illumina). Illumina HiSeq 4000 gds 305658930 GSM5658930 GEO Accession GSM5658930 SRX12798393 GSM5658931 SRP343427 SRS10744153 GSM5658931 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol protocol, followed by DNase treatment. RNA was then re-purified with an aqueous column-based protocol followed by gel analysis to analyze purity and quality of the RNA. The RNAseq libraries were prepared with Illumina's 'TruSeq Stranded mRNAseq Sample Prep kit' (Illumina). Read 1 aligns to the ANTISENSE strand and Read 2 aligns to the SENSE strand. * The libraries were quantitated by qPCR and sequenced on two lanes for 101 cycles from one end of the fragments on a HiSeq 4000 using a HiSeq 4000 sequencing kit version 1. Fastq files were generated and demultiplexed with with the bcl2fastq v2.17.1.14 Conversion Software (Illumina). Illumina HiSeq 4000 gds 305658931 GSM5658931 GEO Accession GSM5658931 SRX12798394 GSM5658932 SRP343427 SRS10744154 GSM5658932 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol protocol, followed by DNase treatment. RNA was then re-purified with an aqueous column-based protocol followed by gel analysis to analyze purity and quality of the RNA. The RNAseq libraries were prepared with Illumina's 'TruSeq Stranded mRNAseq Sample Prep kit' (Illumina). Read 1 aligns to the ANTISENSE strand and Read 2 aligns to the SENSE strand. * The libraries were quantitated by qPCR and sequenced on two lanes for 101 cycles from one end of the fragments on a HiSeq 4000 using a HiSeq 4000 sequencing kit version 1. Fastq files were generated and demultiplexed with with the bcl2fastq v2.17.1.14 Conversion Software (Illumina). Illumina HiSeq 4000 gds 305658932 GSM5658932 GEO Accession GSM5658932 SRX12798395 GSM5658933 SRP343427 SRS10744155 GSM5658933 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol protocol, followed by DNase treatment. RNA was then re-purified with an aqueous column-based protocol followed by gel analysis to analyze purity and quality of the RNA. The RNAseq libraries were prepared with Illumina's 'TruSeq Stranded mRNAseq Sample Prep kit' (Illumina). Read 1 aligns to the ANTISENSE strand and Read 2 aligns to the SENSE strand. * The libraries were quantitated by qPCR and sequenced on two lanes for 101 cycles from one end of the fragments on a HiSeq 4000 using a HiSeq 4000 sequencing kit version 1. Fastq files were generated and demultiplexed with with the bcl2fastq v2.17.1.14 Conversion Software (Illumina). Illumina HiSeq 4000 gds 305658933 GSM5658933 GEO Accession GSM5658933 SRX12798396 GSM5658934 SRP343427 SRS10744156 GSM5658934 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol protocol, followed by DNase treatment. RNA was then re-purified with an aqueous column-based protocol followed by gel analysis to analyze purity and quality of the RNA. The RNAseq libraries were prepared with Illumina's 'TruSeq Stranded mRNAseq Sample Prep kit' (Illumina). Read 1 aligns to the ANTISENSE strand and Read 2 aligns to the SENSE strand. * The libraries were quantitated by qPCR and sequenced on two lanes for 101 cycles from one end of the fragments on a HiSeq 4000 using a HiSeq 4000 sequencing kit version 1. Fastq files were generated and demultiplexed with with the bcl2fastq v2.17.1.14 Conversion Software (Illumina). Illumina HiSeq 4000 gds 305658934 GSM5658934 GEO Accession GSM5658934 SRX12798397 GSM5658935 SRP343427 SRS10744157 GSM5658935 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol protocol, followed by DNase treatment. RNA was then re-purified with an aqueous column-based protocol followed by gel analysis to analyze purity and quality of the RNA. The RNAseq libraries were prepared with Illumina's 'TruSeq Stranded mRNAseq Sample Prep kit' (Illumina). Read 1 aligns to the ANTISENSE strand and Read 2 aligns to the SENSE strand. * The libraries were quantitated by qPCR and sequenced on two lanes for 101 cycles from one end of the fragments on a HiSeq 4000 using a HiSeq 4000 sequencing kit version 1. Fastq files were generated and demultiplexed with with the bcl2fastq v2.17.1.14 Conversion Software (Illumina). Illumina HiSeq 4000 gds 305658935 GSM5658935 GEO Accession GSM5658935 SRX12798398 GSM5658936 SRP343427 SRS10744158 GSM5658936 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol protocol, followed by DNase treatment. RNA was then re-purified with an aqueous column-based protocol followed by gel analysis to analyze purity and quality of the RNA. The RNAseq libraries were prepared with Illumina's 'TruSeq Stranded mRNAseq Sample Prep kit' (Illumina). Read 1 aligns to the ANTISENSE strand and Read 2 aligns to the SENSE strand. * The libraries were quantitated by qPCR and sequenced on two lanes for 101 cycles from one end of the fragments on a HiSeq 4000 using a HiSeq 4000 sequencing kit version 1. Fastq files were generated and demultiplexed with with the bcl2fastq v2.17.1.14 Conversion Software (Illumina). Illumina HiSeq 4000 gds 305658936 GSM5658936 GEO Accession GSM5658936